A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277976



Internal ID20845016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39890924..39891761hg38UCSC Ensembl
chr8:39748443..39749280hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558900
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277976
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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